US4490525AExpiredUtility

Polysaccharides containing phthalocyanine nucleus

Assignee: SUMITOMO CHEMICAL COPriority: Jul 1, 1982Filed: Jul 1, 1982Granted: Dec 25, 1984
Est. expiryJul 1, 2002(expired)· nominal 20-yr term from priority
G01N 33/548C08B 37/0039C07F 19/005C08B 31/00C07F 1/005
40
PatentIndex Score
8
Cited by
4
References
13
Claims

Abstract

Metal-containing or metal-free phthalocyanine-polysaccharide complex defined below is used for removal of mutagens and carcinogens present in aqueous solutions, the said complex having formula of ##STR1## wherein Pc is a metal-containing or metal-free phthalocyanine residue, A is an alkylene group having 2 to 6 carbon atoms or an arylene group having 1 to 3 rings, the integers m and n satisfy both 2<m+n≦4 and 1≦n≦2, and Z is an activated polysaccharide residue.

Claims

exact text as granted — not AI-modified
We claim: 
     
       1. A phthalocyanine-polysaccharide complex represented by the formula, when it is shown as a free acid, ##STR4## wherein Pc is a copper, iron, nickel, cobalt or aluminum containing or metal-free phthalocyanine residue; A is an alkylene group having 2 to 6 carbon atoms or an arylene group having 1 to 3 rings; m and n are integers satisfying both the 2<m+n≦4 and 1≦n≦2 equations; and Z is an activated polysaccharide residue selected from the group consisting of agarose and dextrin. 
     
     
       2. A phthalocyanine-polysaccharide complex according to claim 1, which has the formula, when it is shown in the free acid, ##STR5## wherein CuPc is copper phthalocyanine residue and Z, m and n are the same as defined in claim 1. 
     
     
       3. A process for preparing a phthalocyanine-polysaccharide complex formula, when it is shown in the free acid, ##STR6## wherein Pc is a copper, iron, nickel, cobalt or aluminum containing or metal-free phthalocyanine residue; A is an alkylene group having 2 to 6 carbon atoms or an arylene group having 1 to 3 rings; m and n are integers satisfying both the 2<M+n≦4 and 1≦n≦2 equations; and Z is an activated polysaccharide residue selected from the group consisting of agarose and dextrin which comprises coupling activated polysaccharide with a water-soluble compound, as the ligand, represented by the general formula, when it is shown as the free acid, ##STR7## 
     
     
       4. A method for removal of mutagens from aqueous solution, comprising adsorbing the mutagen in aqueous solution by using a phthalocyanine-polysaccharide complex represented by the formula, when it is shown as the free acid, ##STR8## wherein Pc is a copper, iron, nickel, cobalt or aluminum containing or metal-free phthalocyanine residue; A is an alkylene group having 2 to 6 carbon atoms or an arylene group having 1 to 3 rings; m and n are integers satisfying both the 2<m+n≦4 and 1≦n≦2 equations; and Z is an activated polysaccharide residue selected from the group consisting of agarose and dextrin. 
     
     
       5. A phthalocyanine-polysaccharide complex according to claim 1 wherein the activated polysaccharide residue is a residue of agarose. 
     
     
       6. A phthalocyanine-polysaccharide complex according to claim 2 wherein the activated polysaccharide residue is a residue of agarose. 
     
     
       7. A method according to claim 4 wherein the activated polysaccharide residue is a residue of agarose. 
     
     
       8. A phthalocyanine-polysaccharide complex according to claim 1 wherein the activation had been carried out with cyanogen bromide. 
     
     
       9. A phthalocyanene-polysaccharide complex according to claim 2 wherein the activation had been carried out with cyanogen bromide. 
     
     
       10. A process according to claim 3 wherein the activation had been carried out with cyanogen chloride. 
     
     
       11. A method according to claim 4 wherein the activation had been carried out with cyanogen bromide. 
     
     
       12. A method according to claim 4 including the additional step of eluting the mutagen. 
     
     
       13. A method according to claim 12 wherein the activation had been carried out with cyanogen bromide.

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